Zhan Lei, Yang Li J, Huang Yu, He Qing, Liu Guan J
Department of Neurosurgery, The First People's Hospital of Shuangliu County, Chengdu, China, 610041.
Emergency Department, Affiliated Hospital of Chengdu University, Chengdu, Sichuan, China, 610081.
Cochrane Database Syst Rev. 2017 Mar 27;3(3):CD010134. doi: 10.1002/14651858.CD010134.pub2.
Out-of-hospital cardiac arrest (OHCA) is a major cause of death worldwide. Cardiac arrest can be subdivided into asphyxial and non asphyxial etiologies. An asphyxia arrest is caused by lack of oxygen in the blood and occurs in drowning and choking victims and in other circumstances. A non asphyxial arrest is usually a loss of functioning cardiac electrical activity. Cardiopulmonary resuscitation (CPR) is a well-established treatment for cardiac arrest. Conventional CPR includes both chest compressions and 'rescue breathing' such as mouth-to-mouth breathing. Rescue breathing is delivered between chest compressions using a fixed ratio, such as two breaths to 30 compressions or can be delivered asynchronously without interrupting chest compression. Studies show that applying continuous chest compressions is critical for survival and interrupting them for rescue breathing might increase risk of death. Continuous chest compression CPR may be performed with or without rescue breathing.
To assess the effects of continuous chest compression CPR (with or without rescue breathing) versus conventional CPR plus rescue breathing (interrupted chest compression with pauses for breaths) of non-asphyxial OHCA.
We searched the Cochrane Central Register of Controlled Trials (CENTRAL; Issue 1 2017); MEDLINE (Ovid) (from 1985 to February 2017); Embase (1985 to February 2017); Web of Science (1985 to February 2017). We searched ongoing trials databases including controlledtrials.com and clinicaltrials.gov. We did not impose any language or publication restrictions.
We included randomized and quasi-randomized studies in adults and children suffering non-asphyxial OHCA due to any cause. Studies compared the effects of continuous chest compression CPR (with or without rescue breathing) with interrupted CPR plus rescue breathing provided by rescuers (bystanders or professional CPR providers).
Two authors extracted the data and summarized the effects as risk ratios (RRs), adjusted risk differences (ARDs) or mean differences (MDs). We assessed the quality of evidence using GRADE.
We included three randomized controlled trials (RCTs) and one cluster-RCT (with a total of 26,742 participants analysed). We identified one ongoing study. While predominantly adult patients, one study included children. Untrained bystander-administered CPRThree studies assessed CPR provided by untrained bystanders in urban areas of the USA, Sweden and the UK. Bystanders administered CPR under telephone instruction from emergency services. There was an unclear risk of selection bias in two trials and low risk of detection, attrition, and reporting bias in all three trials. Survival outcomes were unlikely to be affected by the unblinded design of the studies.We found high-quality evidence that continuous chest compression CPR without rescue breathing improved participants' survival to hospital discharge compared with interrupted chest compression with pauses for rescue breathing (ratio 15:2) by 2.4% (14% versus 11.6%; RR 1.21, 95% confidence interval (CI) 1.01 to 1.46; 3 studies, 3031 participants).One trial reported survival to hospital admission, but the number of participants was too low to be certain about the effects of the different treatment strategies on survival to admission(RR 1.18, 95% CI 0.94 to 1.48; 1 study, 520 participants; moderate-quality evidence).There were no data available for survival at one year, quality of life, return of spontaneous circulation or adverse effects.There was insufficient evidence to determine the effect of the different strategies on neurological outcomes at hospital discharge (RR 1.25, 95% CI 0.94 to 1.66; 1 study, 1286 participants; moderate-quality evidence). The proportion of participants categorized as having good or moderate cerebral performance was 11% following treatment with interrupted chest compression plus rescue breathing compared with 10% to 18% for those treated with continuous chest compression CPR without rescue breathing. CPR administered by a trained professional In one trial that assessed OHCA CPR administered by emergency medical service professionals (EMS) 23,711 participants received either continuous chest compression CPR (100/minute) with asynchronous rescue breathing (10/minute) or interrupted chest compression with pauses for rescue breathing (ratio 30:2). The study was at low risk of bias overall.After OHCA, risk of survival to hospital discharge is probably slightly lower for continuous chest compression CPR with asynchronous rescue breathing compared with interrupted chest compression plus rescue breathing (9.0% versus 9.7%) with an adjusted risk difference (ARD) of -0.7%; 95% CI (-1.5% to 0.1%); moderate-quality evidence.There is high-quality evidence that survival to hospital admission is 1.3% lower with continuous chest compression CPR with asynchronous rescue breathing compared with interrupted chest compression plus rescue breathing (24.6% versus 25.9%; ARD -1.3% 95% CI (-2.4% to -0.2%)).Survival at one year and quality of life were not reported.Return of spontaneous circulation is likely to be slightly lower in people treated with continuous chest compression CPR plus asynchronous rescue breathing (24.2% versus 25.3%; -1.1% (95% CI -2.4 to 0.1)), high-quality evidence.There is high-quality evidence of little or no difference in neurological outcome at discharge between these two interventions (7.0% versus 7.7%; ARD -0.6% (95% CI -1.4 to 0.1).Rates of adverse events were 54.4% in those treated with continuous chest compressions plus asynchronous rescue breathing versus 55.4% in people treated with interrupted chest compression plus rescue breathing compared with the ARD being -1% (-2.3 to 0.4), moderate-quality evidence).
AUTHORS' CONCLUSIONS: Following OHCA, we have found that bystander-administered chest compression-only CPR, supported by telephone instruction, increases the proportion of people who survive to hospital discharge compared with conventional interrupted chest compression CPR plus rescue breathing. Some uncertainty remains about how well neurological function is preserved in this population and there is no information available regarding adverse effects.When CPR was performed by EMS providers, continuous chest compressions plus asynchronous rescue breathing did not result in higher rates for survival to hospital discharge compared to interrupted chest compression plus rescue breathing. The results indicate slightly lower rates of survival to admission or discharge, favourable neurological outcome and return of spontaneous circulation observed following continuous chest compression. Adverse effects are probably slightly lower with continuous chest compression.Increased availability of automated external defibrillators (AEDs), and AED use in CPR need to be examined, and also whether continuous chest compression CPR is appropriate for paediatric cardiac arrest.
院外心脏骤停(OHCA)是全球主要的死亡原因。心脏骤停可细分为窒息性和非窒息性病因。窒息性心脏骤停是由血液中缺氧引起的,发生在溺水、窒息受害者及其他情况下。非窒息性心脏骤停通常是心脏电活动功能丧失。心肺复苏(CPR)是治疗心脏骤停的既定方法。传统心肺复苏包括胸外按压和“人工呼吸”,如口对口呼吸。人工呼吸在胸外按压期间按固定比例进行,如每30次按压进行2次呼吸,也可在不中断胸外按压的情况下异步进行。研究表明,持续胸外按压对生存至关重要,而中断胸外按压进行人工呼吸可能会增加死亡风险。持续胸外按压心肺复苏可在有或没有人工呼吸的情况下进行。
评估非窒息性院外心脏骤停时持续胸外按压心肺复苏(有或没有人工呼吸)与传统心肺复苏加人工呼吸(中断胸外按压并暂停进行呼吸)的效果。
我们检索了Cochrane对照试验中心注册库(CENTRAL;2017年第1期);MEDLINE(Ovid)(1985年至2017年2月);Embase(1985年至2017年2月);科学网(1985年至2017年2月)。我们检索了正在进行的试验数据库,包括controlledtrials.com和clinicaltrials.gov。我们未施加任何语言或出版限制。
我们纳入了因任何原因导致非窒息性院外心脏骤停的成人和儿童的随机及半随机研究。研究比较了持续胸外按压心肺复苏(有或没有人工呼吸)与救援者(旁观者或专业心肺复苏提供者)进行的中断心肺复苏加人工呼吸的效果。
两位作者提取数据,并将效果总结为风险比(RRs)、调整风险差(ARDs)或均值差(MDs)。我们使用GRADE评估证据质量。
我们纳入了三项随机对照试验(RCTs)和一项整群随机对照试验(共分析了26,742名参与者)。我们确定了一项正在进行的研究。虽然主要是成年患者,但有一项研究纳入了儿童。未经培训的旁观者实施的心肺复苏三项研究评估了美国、瑞典和英国城市地区未经培训的旁观者实施的心肺复苏。旁观者在紧急服务机构的电话指导下实施心肺复苏。两项试验存在选择偏倚风险不明确,所有三项试验的检测、失访和报告偏倚风险较低。生存结局不太可能受到研究非盲法设计的影响。我们发现高质量证据表明,与中断胸外按压并暂停进行人工呼吸(比例15:2)相比,不进行人工呼吸的持续胸外按压心肺复苏可使参与者存活至出院的比例提高2.4%(14%对11.6%;RR 1.21,95%置信区间(CI)1.01至1.46;3项研究,3031名参与者)。一项试验报告了存活至入院情况,但参与者数量过少,无法确定不同治疗策略对存活至入院的影响(RR 1.18,95% CI 0.94至1.48;1项研究,520名参与者;中等质量证据)。没有关于一年生存率、生活质量、自主循环恢复或不良反应的数据。没有足够的证据确定不同策略对出院时神经学结局的影响(RR 1.25,95% CI 0.94至1.66;1项研究,1286名参与者;中等质量证据)。中断胸外按压加人工呼吸治疗后,被归类为具有良好或中等脑功能表现的参与者比例为11%,而不进行人工呼吸的持续胸外按压心肺复苏治疗的参与者比例为1%至18%。由训练有素的专业人员实施的心肺复苏在一项评估紧急医疗服务专业人员(EMS)实施的院外心脏骤停心肺复苏的试验中,23,711名参与者接受了持续胸外按压心肺复苏(每分钟100次)并异步进行人工呼吸(每分钟10次)或中断胸外按压并暂停进行人工呼吸(比例30:2)。该研究总体偏倚风险较低。院外心脏骤停后,与中断胸外按压加人工呼吸相比,持续胸外按压并异步进行人工呼吸的存活至出院风险可能略低(9.0%对9.7%),调整风险差(ARD)为-0.7%;95% CI(-1.5%至0.1%);中等质量证据。有高质量证据表明,与中断胸外按压加人工呼吸相比,持续胸外按压并异步进行人工呼吸的存活至入院率低1.3%(24.6%对25.9%;ARD -1.3% 95% CI(-2.4%至-0.2%))。未报告一年生存率和生活质量。持续胸外按压并异步进行人工呼吸治疗的患者自主循环恢复可能略低(24.2%对25.3%;-1.1%(95% CI -2.4至0.1)),高质量证据。有高质量证据表明,这两种干预措施出院时神经学结局几乎没有差异(7.0%对7.7%;ARD -0.6%(95% CI -1.4至0.1))。持续胸外按压加异步人工呼吸治疗的不良事件发生率为54.4%,中断胸外按压加人工呼吸治疗的不良事件发生率为55.4%,调整风险差为-1%(-2.3至0.4),中等质量证据)。
院外心脏骤停后,我们发现旁观者在电话指导下进行仅胸外按压的心肺复苏,与传统的中断胸外按压加人工呼吸相比,可提高存活至出院的人数比例。该人群神经功能的保留情况仍存在一些不确定性,且没有关于不良反应的信息。当由紧急医疗服务人员进行心肺复苏时,与中断胸外按压加人工呼吸相比,持续胸外按压并异步进行人工呼吸并未导致更高的存活至出院率。结果表明,持续胸外按压后观察到的存活至入院或出院率略低、神经学结局良好和自主循环恢复。持续胸外按压的不良反应可能略低。需要研究自动体外除颤器(AED)的可用性增加以及在心肺复苏中使用AED的情况,以及持续胸外按压心肺复苏是否适用于小儿心脏骤停。